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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749174Generated: October 30, 2026

Acetic Acid → (3-([7-(4-chlorobutoxy)-6-methoxyquinazolin-4-yl]amino)-1H-pyrazol-5-yl)acetic acid

https://huagongshe.com/reaction/749174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant(5-Amino-2H-pyrazol-3-yl)-acetic acidHCID 16221512—
ReactantN'-[5-(4-chlorobutoxy)-2-cyano-4-methoxyphenyl]-N,N-dimethylimidoformamideHCID 68993086—
SolventEthanolHCID 702—
Product(3-([7-(4-chlorobutoxy)-6-methoxyquinazolin-4-yl]amino)-1H-pyrazol-5-yl)acetic acidHCID 6898781774%

Reaction Steps

N′-[5-(4-chlorobutoxy)-2-cyano-4-methoxyphenyl]-N,N-dimethylimidoformamide (464 g, 15 mmol) in acetic acid (13.5 ml, 225 mmol) was reacted with (3-amino-1H-pyrazol-5-yl)acetic acid (2.22 g, 15.8 mmol) at reflux for 1 hour. The mixture was cooled, diluted with ethanol (25 ml) and the resultant precipitate recovered by suction filtration. The solid was stirred in water for 1 hour, collected by suction filtration and dried to yield (3-([7-(4-chlorobutoxy)-6-methoxyquinazolin-4-yl]amino)-1H-pyrazol-5-yl)acetic acid (4.5 g, 74% yield):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402585B2
Source datasetuspto-grants-2008_07
ORD IDord-2233b8fd53f14bc9a72fceef8ef92455
Source noteuspto-grants-2008_07